Online "Pain, Stress & Emotions" Class in Chronic Pain

Early Phase 1

Completed

• Conditions: Chronic Pain
• Interventions: Behavioral: Pain, Stress and Emotions

• Registration Number: NCT05014126
• Lead Sponsor: Stanford University

Brief Summary

Members with chronic pain will be invited to participate in a 2-hour zoom-delivered pain psychology class entitled "Pain, Stress, \& Emotions". Surveys are completed at baseline (prior to the online class), a satisfaction survey is completed after the class, and post-treatment surveys completed 2, 4, 8, and 12 1weeks after class attendance.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2021-08-12
• Study First Submitted QC: 2021-08-18
• Study Start: 2021-08-20
• Study First Posted: 2021-08-20
• Primary Completion: 2022-01-15
• Study Completion: 2022-03-20
• Status Verified: 2024-11
• Last Update Submitted: 2024-11-04
• Last Update Posted: 2024-11-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 74

Inclusion Criteria

• Chronic pain condition (pain > 3 months)
• Access to the internet
• English fluency

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Exclusion Criteria

• Ongoing legal action or disability claim
• Cognitive impairment, non-English speaking, or psychological factors that would preclude comprehension of material and/or full participation in the study.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Pain, Stress, & Emotions Class	Pain, Stress and Emotions	No active or placebo comparator will be used. This is a single-arm study design.

Primary Outcome Measures

Name	Time	Method
Pain Intensity NRS	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	Self-reported pain intensity rating

Secondary Outcome Measures

Name	Time	Method
Patient-Reported Outcomes Measurement Information System: Pain Interference short form 6a	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	self-reported pain interference levels
Patient-Reported Outcomes Measurement Information System: Depression 6a	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	self-reported depression
Patient-Reported Outcomes Measurement Information System: Anxiety 6a	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	self-reported anxiety
Patient-Reported Outcomes Measurement Information System: Physical Function 8b	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	self-reported physical functioning
Patient-Reported Outcomes Measurement Information System: Sleep Disturbance 6a	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	self-reported sleep disturbance
Patient-Reported Outcomes Measurement Information System: social isolation 6a	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	self-reported social isolation
Patient-Reported Outcomes Measurement Information System: fatigue 6a	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	self-reported fatigue
Patient-Reported Outcomes Measurement Information System: anger 5a	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	self-reported anger
Ambivalence over Emotional Expression (AEQ)	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	self-reported ambivalence levels about emotional expression
Emotion-Approach Coping	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	8-item emotion approach coping scale
Pain Bothersomeness	Change from baseline to 1-Month follow-up (with secondary 2-month follow-up)	single-item assessing self-reported levels of pain bothersomeness

Trial Locations

Locations (1)

Stanford University; 🇺🇸 Palo Alto, California, United States